CN103140338B - Comprise the pneumatic tire of self-adhesive composite reinforcement - Google Patents
Comprise the pneumatic tire of self-adhesive composite reinforcement Download PDFInfo
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- CN103140338B CN103140338B CN201180045876.2A CN201180045876A CN103140338B CN 103140338 B CN103140338 B CN 103140338B CN 201180045876 A CN201180045876 A CN 201180045876A CN 103140338 B CN103140338 B CN 103140338B
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- Prior art keywords
- styrene
- silk thread
- thermoplastic
- tire
- reinforcing body
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Links
- 230000002787 reinforcement Effects 0.000 title claims abstract description 58
- 239000002131 composite material Substances 0.000 title claims abstract description 52
- 239000000853 adhesive Substances 0.000 title description 18
- 230000003014 reinforcing effect Effects 0.000 claims abstract description 69
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 59
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 53
- 229920001971 elastomer Polymers 0.000 claims abstract description 47
- 239000000203 mixture Substances 0.000 claims abstract description 37
- 239000000806 elastomer Substances 0.000 claims abstract description 32
- 230000009477 glass transition Effects 0.000 claims abstract description 23
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 19
- 229910000975 Carbon steel Inorganic materials 0.000 claims abstract description 6
- 239000010962 carbon steel Substances 0.000 claims abstract description 6
- 239000010410 layer Substances 0.000 claims description 22
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 20
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 14
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 claims description 13
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 10
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 8
- 229920000571 Nylon 11 Polymers 0.000 claims description 7
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 6
- 239000004953 Aliphatic polyamide Substances 0.000 claims description 4
- 229920003231 aliphatic polyamide Polymers 0.000 claims description 4
- 229920001400 block copolymer Polymers 0.000 claims description 4
- 150000001993 dienes Chemical class 0.000 claims description 3
- 229920002292 Nylon 6 Polymers 0.000 claims description 2
- 229920003232 aliphatic polyester Polymers 0.000 claims description 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 claims 1
- 239000002356 single layer Substances 0.000 claims 1
- 229920003244 diene elastomer Polymers 0.000 abstract description 8
- 239000011159 matrix material Substances 0.000 abstract description 6
- 238000007711 solidification Methods 0.000 abstract description 4
- 230000008023 solidification Effects 0.000 abstract description 4
- 230000001070 adhesive effect Effects 0.000 description 17
- 239000011324 bead Substances 0.000 description 17
- 239000005060 rubber Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 13
- 239000004952 Polyamide Substances 0.000 description 12
- 229910000831 Steel Inorganic materials 0.000 description 12
- 239000010959 steel Substances 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229920002647 polyamide Polymers 0.000 description 11
- 239000003981 vehicle Substances 0.000 description 10
- 229920000728 polyester Polymers 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000003351 stiffener Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- -1 polybutylene terephthalate Polymers 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910001369 Brass Inorganic materials 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 229920002633 Kraton (polymer) Polymers 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001868 cobalt Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
- 229920005644 polyethylene terephthalate glycol copolymer Polymers 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 210000001130 astrocyte Anatomy 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000010066 calendering (rubber) Methods 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 238000013441 quality evaluation Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 150000007984 tetrahydrofuranes Chemical group 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D30/00—Producing pneumatic or solid tyres or parts thereof
- B29D30/06—Pneumatic tyres or parts thereof (e.g. produced by casting, moulding, compression moulding, injection moulding, centrifugal casting)
- B29D30/38—Textile inserts, e.g. cord or canvas layers, for tyres; Treatment of inserts prior to building the tyre
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B15/00—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
- B29B15/08—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B15/00—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
- B29B15/08—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
- B29B15/10—Coating or impregnating independently of the moulding or shaping step
- B29B15/12—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length
- B29B15/122—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length with a matrix in liquid form, e.g. as melt, solution or latex
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D30/00—Producing pneumatic or solid tyres or parts thereof
- B29D30/06—Pneumatic tyres or parts thereof (e.g. produced by casting, moulding, compression moulding, injection moulding, centrifugal casting)
- B29D30/38—Textile inserts, e.g. cord or canvas layers, for tyres; Treatment of inserts prior to building the tyre
- B29D2030/383—Chemical treatment of the reinforcing elements, e.g. cords, wires and filamentary materials, to increase the adhesion to the rubber
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/294—Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Ropes Or Cables (AREA)
- Tires In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
Comprise the pneumatic tire of composite reinforcing body (R-2), described composite reinforcing body is by solidification and diene rubber matrix autoadhesion, and described composite reinforcing body comprises :-one or more reinforcement silk thread (20), such as carbon steel cord; The layer of-thermoplastic polymer composition, its coated described silk thread, the coated several silk thread of coated each silk thread or collectivity ground individually, described thermoplastic polymer composition comprise on the one hand glass transition temperature be on the occasion of thermoplastic polymer, comprise the unsaturated thermoplastic styrene elastomer that glass transition temperature is negative value on the other hand.
Description
Technical field
The field of the invention is for airtyred stiffening members or reinforcing body, especially metal reinforcement body.
The present invention relates more specifically to the pneumatic tire of mixed type or compound reinforcing body reinforcement, described reinforcing body is by least one core body, particularly metallic core is formed, and described core body is covered (sheath) by the sheath coated (cover) of one deck thermoplastic or a thermoplastic or cover.
Background technology
Use thermoplastic; such as polyamide or polyester are as the sheath known considerable time of metal reinforcement body; particularly be used for protecting these reinforcing body not corrode by polytype outside; such as oxidation or wearing and tearing; or for the object of structure rigidifying; by all kinds of silk thread (thread) or silk thread assembly such as cord (cord) being bonded together, and improve their resistance to bending thus especially.
Such composite reinforcing body and their purposes in rubber such as pneumatic tire have been described in many patent documents.
Such as, patent application EP0962562 describes the reinforcing body be made up of steel or kevlar fabric, and for improving its object of wearability, it is covered by thermoplastic such as polyester or polyamide cover.
Patent application FR2601293 describes with the sheath of polyamide as metal cords, and it to be used as the bead in pneumatic tire tyre bead, such sheath advantageously makes the shape of this bead be applicable to structure and the condition of work of the pneumatic tire tyre bead of its reinforcement.
Patent document FR2576247 and US4,754,794 also illustrate metal cords or tinsel, it can be used as the bead in pneumatic tire tyre bead, these silk threads or cord by two kinds or even three kinds of different thermoplastic material (such as polyamide) double braid coverings with different melting points to cover or even three layers of cover cover, its object is control the distance between these silk threads or cord on the one hand, and be the risk eliminating friction loss or corrosion losses on the other hand, they to be used as the bead in pneumatic tire tyre bead.
Use these reinforcing body that polyester or polyamide material cover cover thus except the advantage of above-mentioned corrosion resistance, wearability and structural rigidity, their important advantages use the simple textile binding agent being called as RFL (Resorcin-Formaldehyde-Latex) adhesive to bond with diene rubber matrix subsequently, described diene rubber matrix comprises at least one diene elastomer such as natural rubber, described adhesive is known can provide fabric fibre, such as polyester or gratifying bonding between Fypro and diene rubber.
Therefore, use the metal reinforcement body not being coated with adhesion metal layer such as brass, and it may be favourable that use does not contain metallic salts such as the rubber matrix of the surrounding of cobalt salt, described slaine known for maintenance through time cohesive be necessary, but it significantly increases the cost of rubber matrix itself on the one hand, and increase their oxidation and ageing sensitivity (see such as patent application WO2005/113666) on the other hand.
But above RFL adhesive also has shortcoming: particularly they comprise formaldehyde as base material, due to the current change in the European directive about the type product, formaldehyde is the material being hoped to remove from adhesive composition on long terms.
Therefore, pneumatic tire manufacturer is seeking to alleviate the new adhesive system of above-mentioned all or part shortcoming or new reinforcing body at present.
Summary of the invention
At present, applicant has found a kind of composite reinforcing body in its process studied, and it does not need applying glue process to come and rubber adhesion, be the type by solidifying autoadhesion, and therefore it can make above-mentioned purpose be achieved under certain meaning.
Therefore, the first theme of the present invention is the pneumatic tire comprising composite reinforcing body, and described composite reinforcing body comprises:
-one or more reinforcement silk thread;
The layer of-thermoplastic polymer composition, its coated described silk thread, the coated several silk thread of coated each silk thread or collectivity ground individually, described thermoplastic polymer composition comprise on the one hand glass transition temperature be on the occasion of thermoplastic polymer, comprise the unsaturated thermoplastic styrene elastomer that glass transition temperature is negative value on the other hand.
Unexpectedly, found the existence of this unsaturated thermoplastic styrene elastomer make likely to guarantee described composite reinforcing body directly (namely not containing RFL adhesive or other adhesive any) and securely with diene elastomer matrix or composition, be such as widely used in those compositions bonding in tire.
The invention still further relates to the purposes of above-mentioned composite reinforcing body as stiffening members, described stiffening members is used for pneumatic tire, especially wish to be arranged on passenger car type automobile, SUVs (" sport utility vehicle "), two wheeler (particularly bicycle or motorcycle), aircraft or industrial vehicle, it is selected from van, " heavy type " vehicle, i.e. underground train, bus, heavy road surface haulage vehicle (truck, tractor, trailer), non-road vehicles such as agricultural machinery or civil engineering machine, and other transport or operate those tires on vehicle.
According to the following description and embodiment, and the accompanying drawing schematically shown combining these embodiments relevant will easily understand the present invention and advantage thereof:
-Fig. 1 display is applicable to the cross section of an example of airtyred composite reinforcing body of the present invention;
-Fig. 2 display is applicable to the cross section of another example of airtyred reinforcing body of the present invention;
-Fig. 3 display is applicable to the cross section of another example of airtyred reinforcing body of the present invention;
-Fig. 4 display is applicable to the cross section of another example of airtyred reinforcing body of the present invention; With
-Fig. 5 shows the airtyred radial section according to present invention adds this composite reinforcing body with radial carcass reinforcement.
Detailed description of the invention
In this manual, unless otherwise its place's explanation, all percentage (%) represents percentage by weight.
In addition, represented from being greater than a by statement " between a-b " any codomain of defining and (namely do not comprise end value a and b), and any codomain defined by statement " a-b " represents from a until the codomain of b (namely comprises accurate end value a and b) to the codomain being less than b.
The airtyred composite reinforcing body of the present invention can by solidification directly and unsaturated rubber composition bond, therefore there is following principal character:
-at least one reinforcement silk thread (i.e. one or more reinforcement silk thread);
The layer of-thermoplastic polymer composition, it is coated described silk thread individually, and the coated several silk thread of coated each silk thread or collectivity ground, described thermoplastic polymer composition comprises glass transition temperature (hereinafter referred to as Tg on the one hand
1) on the occasion of (being namely greater than 0 DEG C) thermoplastic polymer, on the other hand comprise glass transition temperature (hereinafter referred to as Tg
2) be the unsaturated thermoplastic styrene elastomer of negative value (being namely less than 0 DEG C).
That is, this composite reinforcing body comprises single reinforcement silk thread or several reinforcement silk thread, each reinforcement silk thread by the layer (individual layer) of thermoplastic polymer composition or sheath institute coated.The structure of this reinforcing body is hereafter being described in detail.
In this application, term " reinforcement silk thread " is generally understood as any elongated member representing and have greater depth relative to its cross section, the no matter shape of its cross section, such as circle, ellipse, rectangle, square or or even flat, this silk thread can also be straight or not be straight, such as, be torsion or corrugated.
This reinforcement silk thread can adopt any known form.Such as, it can be major diameter (such as, and be preferably equal to or greater than 50 μm) independent monofilament (monofilament), independently bar, multifilament fiber (has minor diameter by several, usually independent long filament (filament) composition of 30 μm is less than), by several twisting (twisted) processbearing astrocyte fabric stock yarn together, by also twisting with the fingers (cabled) or twisting several fiber together or meristogenetic fabric or metal curtain line or belt or bar, described band or bar comprise together in groups, along Main way arrangement be no matter whether such as directly to several such monofilament, fiber, stock yarn or cord.
The diameter of described reinforcement silk thread or each reinforcement silk thread is preferably less than 5mm, especially in the scope of 0.1-2mm.
Preferably, described reinforcement silk thread is metal reinforcement silk thread, particularly carbon steel wire, such as, be used in those in tire steel cord.But, certainly can use the steel of other types, as stainless steel.When use carbon steel time, its carbon content preferably between 0.4%-1.2%, particularly between 0.5%-1.1%.The present invention is specially adapted to have any steel of steel cord type of standard or NT (" conventional stretch ") intensity, height or HT (" high stretching ") intensity, very high or SHT (" Ultra-Drawing ") intensity or high or UHT (" high stretching ") intensity.
Described steel can be coated with adhesive phase, such as layer of brass or zinc layers.But, also can advantageously use light, namely uncoated steel.In addition, according to the present invention, wish the rubber composition by metal reinforcement reinforcement body of the present invention, no longer need to use metallic salts as cobalt salt in its formula.
First the thermoplastic polymer composition forming above-mentioned layer or sheath comprises thermoplastic polymer, and it has positive Tg (with Tg according to definition
1represent), it is preferably greater than+20 DEG C, and more preferably greater than+30 DEG C.In addition, the fusing point (claiming to represent with Tm) of this thermoplastic polymer is preferably greater than 100 DEG C, more preferably greater than 150 DEG C, and is greater than 200 DEG C especially.
This thermoplastic polymer is preferably selected from polyamide, polyester and polyimides, is more specifically selected from aliphatic polyamide and polyester.In the polyester, PET (PETG), PEN (PEN), PBT (polybutylene terephthalate (PBT)), PBN (PBN), PPT (PTT) and PPN (poly-naphthalenedicarboxylic acid propylene glycol ester) can such as be mentioned.In aliphatic polyamide, polyamide 4 can be mentioned especially, 6,6,6,6,11 and 12.This thermoplastic polymer is preferably aliphatic polyamide, is more preferably polyamide 6 or polyamide 11.
Second key component of thermoplastic polymer composition is unsaturated thermoplastic styrene elastomer, and it has negative Tg (Tg according to definition
2) value, it is preferably less than-20 DEG C, and is more preferably less than-30 DEG C.
Therefore and according to the preferred embodiments of the invention, described thermoplastic polymer and the elastomeric glass transition temperature difference of unsaturated TPS (Tg
1-Tg
2) be greater than 40 DEG C, more preferably greater than 60 DEG C.
Here should notice that TPS (thermoplastic styrene) elastomer is the thermoplastic elastomer (TPE) of styrene-based block copolymer form.These thermoplastic elastomer (TPE)s between thermoplastic polymer and elastomer with intermediate structure are known is connected by polystyrene hard segment by elastomer soft chain segment (as polybutadiene, polyisoprene or poly-(ethylene/butylene)) sequence and formed.
Known this is the reason that TPS copolymer is characterized by existence two glass transition peaks usually, first (lower, negative temperature, corresponding Tg
2) elastomeric blocks of the corresponding TPS copolymer in peak, and thermoplastic portions's (styrene block) of second corresponding TPS copolymer in (higher, positive temperature, usually at about 80 DEG C) peak.
The elastomer of these TPS elastomers normally three blocks, it has two hard segments connected by soft chain segment.Described hard segment and soft chain segment can arrange in linear form or with star configuration or cladodification structure.These TPS elastomers can also be the diblock elastomers that single hard segment is connected with soft chain segment.Usually, each in these segments or block comprises and is minimumly greater than 5, is generally greater than the base unit (styrene units such as when styrene/isoprene/styrene block copolymer and isoprene unit) of 10.
Draw attention to, the elastomeric essential attributes of the TPS used in composite reinforcing body of the present invention is that it is the undersaturated fact.According to definition, and will state " TPS elastomer " with knowing be interpreted as the TPS elastomer comprising ethylenic unsaturated group, that is, it comprises carbon-to-carbon double bond (no matter whether being conjugation).On the contrary, yes does not comprise the TPS elastomer of such double bond for saturated TPS elastomer.
Preferably, described unsaturated elastic body is the copolymer comprising styrene (i.e. polystyrene) block and diene (i.e. polydiene) block, particularly isoprene (polyisoprene) or butadiene (polybutadiene) block.Such elastomer is selected from phenylethylene/butadiene (SB) especially, styrene/isoprene (SI), styrene/butadiene/butylene (SBB), phenylethylene/butadiene/isoprene (SBI), styrene/butadiene/styrene (SBS), styrene/butadiene/butylene/styrene (SBBS), styrene/isoprene/styrene (SIS), phenylethylene/butadiene/the block copolymer of isoprene/styrene (SBIS) and the blend of these copolymers.
More preferably, this unsaturated elastic body is three block type copolymer, and it is selected from the mixture of styrene/butadiene/styrene (SBS), styrene/butadiene/butylene/styrene (SBBS), styrene/isoprene/styrene (SIS), phenylethylene/butadiene/isoprene/styrene (SBIS) block copolymer and these copolymers; More specifically, it is SBS or SIS, particularly SBS.
According to another preferred embodiment of the present invention, the styrene-content in described unsaturated TPS elastomer is between 5-50%.Outside described scope, technique effect desired by existence is no longer optimum risk, namely trade off relative to the fusible of described thermoplastic polymer layer on the one hand, the fusible of diene elastomer of wishing further relative to described reinforcing body is on the other hand traded off.For those reasons, styrene-content is more preferably between 10-40%.
Elastomeric number-average molecular weight (the M of described TPS
n) preferably at 5000-500000g/mol, more preferably between 7000-450000.In a known way, the elastomeric number-average molecular weight (M of TPS is measured by SEC (size exclusion chromatograph)
n).Sample is first dissolved in oxolane with the concentration being about 1g/L, then before sample introduction, the filter in 0.45 μm of aperture filters this solution.The equipment used is WATERSAlliance chromatograph.Eluting solvent is oxolane, and flow velocity is 0.7ml/min, and system temperature is 35 DEG C, and analysis time is 90min.Tandem ground uses WATERS " STYRAGEL " post (HMW7 post, a HMW6E post and two HT6E posts) of a set of 4.The sampling volume of this polymer samples solution is 100 μ l.Detector is WATERS2410 differential refractometer, and is WATERSMILLENIUM systems for the treatment of the related software of chromatograph data.The mean molecule quantity calculated is the molecular weight relative to the calibration curve using polystyrene standards to obtain.
Unsaturated TPS elastomer as SB, SBS, SBBS, SIS or SBIS be know and can title " KratonD " purchased from Kraton company (product D1161, D1118, D1116, D1163 as in the elastomeric situation of SB, SIS and SBS), can title " Calprene " purchased from Dynasol company (products C 405, C411 and C412 as in the elastomeric situation of SBS), or can title " Tuftec " purchased from Asahi company (product P 1500 as in the elastomeric situation of SBBS).
Glass transition temperature (the Tg of above-mentioned thermoplastic polymer
1and Tg
2) such as and except difference described in this application illustrate, according to ASTMD3418 (1999) standard, by DSC (differential scanning calorimeter), measure in known manner.
The Fig. 1 enclosed show schematically show, and (not according to concrete scale) is applicable to the cross section of the first example of the composite reinforcing body of tire of the present invention.Be made up of reinforcement silk thread (10) with this composite reinforcing body that R-1 represents, described reinforcement silk thread (10) is by having relative major diameter (such as, single long filament 0.10-0.50mm) or monofilament composition, such as be made up of carbon steel, reinforcement silk thread (10) is coated by layer (11), and described layer (11) comprises on the one hand and has positive glass transition temperature (Tg
1) thermoplastic polymer, be such as made up of polyamide or polyester, and comprise on the other hand there is negative glass transition temperature (Tg)
2) unsaturated TPS elastomer, such as SB, SBS, SBBS, SIS or SBIS; The minimum thickness of this layer is in FIG with E
mrepresent.
Fig. 2 schematically shows the cross section of the second example of the composite reinforcing body being applicable to tire of the present invention.Be made up of reinforcement silk thread (20) with this composite reinforcing body that R-2 represents, reinforcement silk thread (20) is in fact by two single long filaments or the monofilament (20a with relative major diameter (such as between 0.10-0.50mm), 20b) twisting or and twist with the fingers form together, it is such as made up of carbon steel.This reinforcement silk thread (20) is by having minimum thickness E
mlayer (21) coated, described layer (21) comprises on the one hand and has positive glass transition temperature (Tg
1) thermoplastic polymer, be such as made up of polyamide or polyester, and comprise on the other hand there is negative glass transition temperature (Tg
2) unsaturated TPS elastomer, such as SB, SBS, SBBS, SIS or SBIS.
Fig. 3 schematically illustrates the cross section of another example of the composite reinforcing body being applicable to tire of the present invention.This composite reinforcing body represented with R-3 is made up of 3 reinforcement silk threads (30), each reinforcement silk thread is by two monofilament (30a with relative major diameter (such as between 0.10-0.50mm), 30b) twisting or and twist with the fingers form together, it is such as made up of steel or carbon.Coated by layer (31) by the assembly that formed of reinforcement silk thread (30) of such as three alignment, described layer (31) comprises on the one hand and has positive glass transition temperature (Tg
1) thermoplastic polymer, be such as made up of polyamide or polyester, and comprise on the other hand there is negative glass transition temperature (Tg
2) unsaturated TPS elastomer, such as SB, SBS, SBBS, SIS or SBIS.
Fig. 4 schematically illustrates the cross section of another example of the composite reinforcing body being applicable to tire of the present invention again.This composite reinforcing body R-4 comprises reinforcement silk thread (40), it is made up of the steel cord of 1+6 structure, its 6 long filaments (41b) having center line or core body line (41a) and have same diameter, described 6 long filaments are spirally wrapped around together around center line.This reinforcement silk thread or cord (40) coated by polymer composition layer (42), described polymer composition comprises polyamide on the one hand, comprises SBS elastomer on the other hand.
Such as, at the composite reinforcing body of tire of the present invention, in those reinforcing body schematically shown in above-mentioned Fig. 1 to 4, around the minimum thickness E of the sheath of one or more reinforcement silk thread
mconcrete working condition of the present invention may be depended on and widely change.It is preferably between 1 μm of-2mm, more preferably between 10 μm of-1mm.
If use several reinforcement silk thread (especially several cord), coating or sheath can be deposited on (especially on each cord) on each reinforcement silk thread individually and (draw attention to, these reinforcement silk threads can or can not be single), it is as such as shown in above-mentioned Fig. 1,2 and 4, or also can be deposited on appropriate (such as aliging along principal direction) several reinforcement silk thread arranged (especially on several cord), it as shown for example in figure 3 collectivity.
The composite reinforcing body of tire of the present invention is prepared by ad hoc approach, described method comprises at least following step, according to this step, cover is carried out at least one (namely one or more) reinforcement silk thread and covers operation, it is preferably through extruder head, to cover with the layer cover of above-mentioned thermoplastic polymer composition, described thermoplastic polymer composition comprises and has positive glass transition temperature (Tg
1) thermoplastic polymer and there is negative glass transition temperature (Tg
2) unsaturated thermoplastic styrene elastomer.
In the manner known to persons skilled in the art, carry out above-mentioned cover to on-line continuous and cover step.Such as, it comprises the die head making described reinforcement silk thread pass through the suitable diameter be heated in the extruder head of proper temperature briefly.
According to preferred embodiment, before passing into extruder head, such as, pass through eddy-current heating or pass through IR radiation by the preheating of one or more described reinforcement silk thread.When leaving this extruder head, such as, use cold air or other gas, or by by described reinforcement silk thread by water-bath and drying steps subsequently, and overlap the one or more reinforcement silk threads covered described in making thus and fully cool, solidify to make polymeric layer.
Therefore the composite reinforcing body obtained can directly be heat-treated alternatively after extrusion or after cooling.
Such as, for obtaining the reinforcement silk thread covered through cover that overall diameter is about 1mm, it is the reinforcement silk thread of about 0.6mm by diameter, be such as the metal cords (illustrating as exemplified in fig. 2) that the independent monofilament of two of 0.3mm is simply formed by the diameter of twisting together, be that the polyamide 11 of about 0.4mm and SBS or SB elastic composition (weight ratio 85/15) are coated with maximum gauge, described extrude/overlap cover production line and comprise two die heads, the diameter of the first die head (reverse die head or upstream die head) is about 0.65mm, and the diameter of the second die head (or downstream die head) is about 0.95mm, two die heads are placed in the extruder head being heated to about 210 DEG C.When covering head with the silk thread speed of service of tens of m/min of the routine under the extruder pump speed of the tens of g/min relative to routine by cover, the polyamide melted at the temperature of 210 DEG C in this extruder and the elastomeric mixture of TPS are coated on described cord.When leaving this cover and covering die head, this cord can be immersed and be filled with in the groove of cold water, to cool before take-up reel passes into oven drying.
Step is covered for above-mentioned cover, before passing into extruder head, advantageously cord (reinforcement silk thread) can be carried out preheating, such as, through by HF generator or pass through heat tunnel.
After this cover covers operation, namely when leaving sheath head, this composite reinforcing body can directly such as by tunnel type baking oven, and such as several meters high, so that wherein through aerial heat treatment.This treatment temperature is such as between 150 DEG C-300 DEG C, according to circumstances through the processing time (such as 10 seconds to 10 minutes) of several seconds to several minutes, it is believed that the duration of the higher process of temperature will be shorter, and heat treatment must not make used thermoplastic remelting or even overbate.The composite reinforcing style of the present invention completed thus as advantageously cooled in atmosphere, to avoid, when being wrapped in last take-up reel, undesirable sticking problem occurs.
In due course, those skilled in the art can know the duration how regulating temperature and above-mentioned optional heating according to concrete operations condition of the present invention, particularly according to the definite character of manufactured composite reinforcing body, particularly according to this process whether in the combination of independent monofilament, the cord be made up of several monofilament or these monofilament or cord, bar such as, carry out.Especially, those skilled in the art can change treatment temperature and processing time easily, make to find by continuous approximation the operating condition giving each specific embodiments optimum adhesion result of the present invention.
The step of method advantageously can be supplemented and be carried out three-dimensional cross-linked last process to reinforcing body as above, to improve the intrinsic cohesiveness of its sheath further, if particularly wish that this composite reinforcing body is finally at relatively-high temperature, use at 100 DEG C.
This is cross-linked and is undertaken by any known method, such as by the bombardment of Physical cross linking methods such as ion or electronics, or pass through Chemical Crosslinking Methods, such as when being extruded, crosslinking agent (as linseed oil) is mixed in this thermoplastic polymer and TPS elastic composition, or by vulcanizing system (i.e. sulfenyl cross-linking system) is mixed in said composition.
The airtyred setting up period of composite reinforcing reinforcement body of the present invention is made in hope, by being present in for the manufacture of the intrinsic cross-linking system in the diene rubber compsns of this tire, and by making this pneumatic tire contact with composite reinforcing body of the present invention, also can be cross-linked.
Above-mentioned composite reinforcing body directly can be used as the stiffening members in pneumatic tire, that is without the need to any additional adhesive composition.Advantageously, it can be used for reinforcement all types vehicle, particularly the pneumatic tire of passenger car type automobile or industrial vehicle such as heavy vehicle.
Such as, the Fig. 5 enclosed show schematically show (not according to special ratios describe) passenger vehicle airtyred radial section of the present invention.
This pneumatic tire 1 comprises by crown stiffener or crown 2, two sidewalls 3 and two tyre beads 4 of being with 6 reinforcement, and each in these tyre beads 4 is by bead 5 reinforcement.Crown 2 there is tyre surface (not showing in this schematic diagram).Carcass reinforcement 7 is wrapped in two bead 5 in each tyre bead 4, and the turning part (upturn) 8 of this stiffener 7, such as towards the outside of tire 1, shows on its wheel rim 9 being arranged on it at this.As is known, carcass reinforcement 7 is made up of at least one cord ply (ply) by cord reinforcement, i.e. so-called " meridian " cord, the cord of such as fabric or metal, that is, these cords are actual to be arranged parallel to each other, and extend to another tyre bead from a tyre bead, make with middle circumferential plane (perpendicular to the plane of tire rotating shaft, it is positioned at the intermediate distance place of two tyre beads 4, and through the centre of crown stiffener 6) in the angle 80 °-90 °.
This pneumatic tire 1 of the present invention such as has the essential feature that at least one crown stiffener or carcass reinforcement comprise composite reinforcing body as above.According to another possible embodiment of the present invention, such as, bead 5 can be become by this composite reinforcing system.
embodiment
the manufacture of test 1-composite reinforcing body
First the composite reinforcing body being applicable to tire of the present invention is manufactured as follows.Initial reinforcement silk thread is pneumatic tire steel cord, and it is made up of standard steel (having the carbon content of 0.7 % by weight), present two diameters be 0.30mm, structure with 1 × 2 of the pitch of 10mm twisting independently silk thread together or monofilament.Cord diameter is 0.6mm.
This cord be extrude-overlap cover on production line by make its by extruder head with polyamide 11 on the one hand (from the RilsenBESNOP40TL of Arkema company; T
mfor about 180 DEG C) and the mixture of SBS or SB (being respectively D1155 and D1118 of Kraton company) on the other hand come coated, described extruder head is heated to 210 DEG C of temperature, and has the upstream die head of two die heads-diameter 0.63mm and the downstream die head of diameter 0.92mm.The thermoplastic mixture be made up of polyamide 11 (pump speed is about 51g/min) and SBS or SB (pump speed is about 9g/min) is heated to 210 DEG C of temperature, and this silk thread (making it be preheated to about 174 DEG C by HF generator) that the speed being therefore coated with 60m/min is run.When leaving cover and covering head, before use air nozzle carries out drying, gained composite reinforcing body runs through the cooling bath being filled with 5 DEG C of water continuously, cools to make its thermoplastic sheath.
The glass transition temperature Tg of the two kinds of polymer more than used
1and Tg
2equal about+45 DEG C respectively (such as, to measure according to following method of operating: 822-2DSC instrument, purchased from MettlerToledo with-95 DEG C; Helium atmosphere, from room temperature (20 DEG C) preheating sample to 100 DEG C (with 20 DEG C/min)), be then cooled to-140 DEG C rapidly, final entry is with the DSC curve of 20 DEG C/min from-140 DEG C to+250 DEG C afterwards.
After this cover covers operation, in these embodiments, by it to be heated to 3m/min the temperature of 270 DEG C under atmospheric environment (air) by tunnel type baking oven, assembly is carried out to the heat treatment of about 100 second time.This produces the composite reinforcing part (the stiffener R-2 schematically shown in Fig. 2) being applicable to tire of the present invention, and it is formed by overlapping with aramid layer and elastomer (SBS or SB) the initial steel cord covered, and its cohesive is best.
In order to determine heat treated optimum operation condition in above test, test 4 processing times (50 seconds, 100 seconds, 200 seconds and 400 seconds) of the temperature range of 160 DEG C-280 DEG C in advance.
the test of test 2-cohesive
Then, by test to the bond quality evaluation between rubber and the composite reinforcing body as above manufactured, in described test, measure from vulcanizate compositions, be also called in vulcanized rubber the power pulled out needed for described reinforcing body.This rubber composition is the conventional composition for extruded metal tire belt cord ply based on natural rubber, carbon black and standard additive.
Described vulcanized rubber is of a size of 200mm × 4.5mm by two, and the jacket body that thickness is 3.5mm is relatively applied in the block rubber (thickness of gained block rubber is 7mm thus) formed together before curing.In the manufacture process of this block rubber, described composite reinforcing body (amounting to 15 strands) by bundle envelope (imprison) between with two of its uncured state sheet rubbers, described composite reinforcing body is spaced, and one end of each composite reinforcing body is all protruded on the both sides of this sheet rubber, and bulge quantity is enough to carry out posterior drawing test.Then the block comprising this reinforcing body is placed in suitable mould, then cure under pressure.Regulate by leave for those skilled in the art ruling solidification temperature and hardening time be suitable for wish test condition.Such as, in this case, described block at 160 DEG C, at the cure under pressure 15 minutes of 16bar.
After solidification, the sample that vulcanized block and 15 bursts of reinforcing body are formed is placed between the fixture of suitable stretching testing machine, with this individually by each reinforcing body under given draw speed and given temperature (such as in this case respectively at 50mm/min and 100 DEG C) tractive go out rubber.By measuring, reinforcing body is pulled out the pullout forces of sample (by F
maxrepresent) (this is the mean value of 15 extension tests) characterize level of adhesion.
It is found that, although in fact not containing RFL adhesive (or other adhesive any), composite reinforcing body of the present invention has and is equivalent to about 52% (SB elastomer) of comparative pullout forces or the high pullout forces F of 57% (SBS elastomer)
max, described comparative pullout forces is only covering with polyamide 11 cover, and the comparative composite reinforcing body using conventional RFL adhesive to bond records, and described high pullout forces forms remarkable result to those skilled in the art.
Under the same conditions, only have polyamide 11 (without SBS elastomer) to overlap and cover and do not show rubber without cohesive (in fact pullout forces is 0) containing the comparative composite reinforcing body of RFL adhesive (or other adhesive any).
Extra test also proves, the use of unsaturated TPS elastomer (SB or SBS), it is not the component being used as cover coating, but as the adhesive (and therefore always contacting with composite reinforcing body) be incorporated in rubber calendering composition, said composition does not provide adhesive effect.
Therefore, due to the level of adhesion of gained, composite reinforcing body of the present invention is because the characteristic of its self adhesion and for using the composite reinforcing body of the thermoplastic prior art of protecting as polyamide or polyester cover (known its needs to use RFL adhesive to guarantee they and rubber adhesion) to be particularly useful and substitute completely reliably.
Claims (14)
1. comprise the pneumatic tire of composite reinforcing body, described composite reinforcing body comprises:
-one or more reinforcement silk thread;
-monolayer thermoplastic polymer composition layer, its coated described silk thread, the coated several silk thread of coated each silk thread or collectivity ground individually, described thermoplastic polymer composition comprise on the one hand glass transition temperature be on the occasion of thermoplastic polymer, comprise the unsaturated thermoplastic styrene elastomer that glass transition temperature is negative value on the other hand.
2. tire according to claim 1, the glass transition temperature of wherein said thermoplastic polymer is higher than+20 DEG C.
3. the tire described in claim 1 or 2, the glass transition temperature of wherein said unsaturated thermoplastic styrene elastomer is lower than-20 DEG C.
4. the tire described in claim 1 or 2, the difference of the glass transition temperature of wherein said thermoplastic polymer and described unsaturated thermoplastic styrene elastomer is greater than 60 DEG C.
5. the tire described in claim 1 or 2, wherein said thermoplastic polymer is aliphatic polyamide or polyester.
6. tire according to claim 5, wherein said thermoplastic polymer is polyamide 6 or polyamide 11.
7. the tire described in claim 1 or 2, wherein said thermoplastic elastomer (TPE) is the copolymer comprising styrene block and diene block.
8. tire according to claim 7, wherein said diene block is isoprene block or butadiene block.
9. tire according to claim 8, wherein said thermoplastic elastomer (TPE) is selected from phenylethylene/butadiene (SB), styrene/isoprene (SI), styrene/butadiene/butylene (SBB), phenylethylene/butadiene/isoprene (SBI), styrene/butadiene/styrene (SBS), styrene/butadiene/butylene/styrene (SBBS), styrene/isoprene/styrene (SIS), the phenylethylene/butadiene/block copolymer of isoprene/styrene (SBIS) and the blend of these copolymers.
10. tire according to claim 9, wherein said thermoplastic elastomer (TPE) is SBS or SIS copolymer.
Tire described in 11. claims 1 or 2, wherein said thermoplastic elastomer (TPE) comprises the styrene between 5-50 % by weight.
Tire described in 12. claims 1 or 2, the minimum thickness of wherein said layer is between 1 μm of-2mm.
Tire described in 13. claims 1 or 2, wherein said reinforcement silk thread is metal wire.
14. tires according to claim 13, wherein said metal wire is carbon steel wire.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1057666A FR2965209B1 (en) | 2010-09-23 | 2010-09-23 | SELF-ADHERENT COMPOSITE REINFORCEMENT |
| FR1057666 | 2010-09-23 | ||
| PCT/EP2011/066113 WO2012038341A1 (en) | 2010-09-23 | 2011-09-16 | Tyre cover comprising a self-adherent composite reinforcement |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103140338A CN103140338A (en) | 2013-06-05 |
| CN103140338B true CN103140338B (en) | 2015-11-25 |
Family
ID=43844600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201180045876.2A Active CN103140338B (en) | 2010-09-23 | 2011-09-16 | Comprise the pneumatic tire of self-adhesive composite reinforcement |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20130280511A1 (en) |
| EP (1) | EP2618976B1 (en) |
| JP (1) | JP6035570B2 (en) |
| KR (1) | KR101798270B1 (en) |
| CN (1) | CN103140338B (en) |
| BR (1) | BR112013005826A8 (en) |
| FR (1) | FR2965209B1 (en) |
| WO (1) | WO2012038341A1 (en) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2967604B1 (en) * | 2010-11-22 | 2012-12-14 | Michelin Soc Tech | SELF-ADHERENT COMPOSITE REINFORCEMENT |
| FR3008997B1 (en) | 2013-07-29 | 2016-01-01 | Michelin & Cie | LOW THICKNESS AND PNEUMATIC REINFORCED PRODUCT COMPRISING THIS PRODUCT |
| FR3008998B1 (en) | 2013-07-29 | 2016-01-01 | Michelin & Cie | LOW THICKNESS AND PNEUMATIC REINFORCED PRODUCT COMPRISING THIS PRODUCT |
| FR3008996B1 (en) | 2013-07-29 | 2016-01-01 | Michelin & Cie | LOW THICKNESS AND PNEUMATIC REINFORCED PRODUCT COMPRISING THIS PRODUCT |
| FR3020369B1 (en) | 2014-04-29 | 2016-05-06 | Michelin & Cie | MULTI-COMPOSITE FLAT REINFORCEMENT |
| FR3027026B1 (en) | 2014-10-13 | 2016-12-09 | Michelin & Cie | REINFORCED PRODUCT COMPRISING A COMPOSITION COMPRISING A RAPID AND PNEUMATIC VULCANIZATION ACCELERATOR COMPRISING SAID REINFORCED PRODUCT |
| FR3027028B1 (en) | 2014-10-13 | 2016-12-09 | Michelin & Cie | REINFORCED PRODUCT COMPRISING A LOW SULFUR AND PNEUMATIC COMPOSITION COMPRISING SAID REINFORCED PRODUCT |
| FR3027027B1 (en) | 2014-10-13 | 2016-12-09 | Michelin & Cie | REINFORCED PRODUCT COMPRISING A COMPOSITION COMPRISING A METAL OXIDE SYSTEM AND A BALANCED AND PNEUMATIC STEARIC ACID DERIVATIVE COMPRISING SAID REINFORCED PRODUCT |
| FR3027025B1 (en) | 2014-10-13 | 2016-12-09 | Michelin & Cie | REINFORCED PRODUCT COMPRISING A LOW SULFUR AND PNEUMATIC COMPOSITION COMPRISING SAID REINFORCED PRODUCT |
| FR3032147B1 (en) | 2015-02-03 | 2017-02-17 | Michelin & Cie | RADIAL TIRE HAVING IMPROVED BELT STRUCTURE |
| FR3032149B1 (en) | 2015-02-03 | 2017-02-17 | Michelin & Cie | RADIAL TIRE HAVING A VERY FINE BELT STRUCTURE |
| FR3036651B1 (en) | 2015-05-28 | 2017-05-19 | Michelin & Cie | MULTI-COMPOSITE FLAT REINFORCEMENT |
| KR102360510B1 (en) | 2015-05-28 | 2022-02-10 | 꽁빠니 제네날 드 에따블리세망 미쉘린 | Multi-composite reinforcement made from improved glass-resin |
| WO2017002872A1 (en) | 2015-06-29 | 2017-01-05 | 株式会社ブリヂストン | Tire and method for manufacturing tire |
| FR3041282B1 (en) | 2015-09-21 | 2017-10-20 | Michelin & Cie | METHOD FOR MANUFACTURING A SHEERED REINFORCING ELEMENT COMPRISING A DEGREASING STEP |
| JP7289300B2 (en) | 2017-12-14 | 2023-06-09 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | Wire guide for producing sheathed reinforcing elements for tires |
| JP7237074B2 (en) | 2017-12-15 | 2023-03-10 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | Method for producing a product reinforced by reinforcing elements |
| EP3728432A1 (en) | 2017-12-19 | 2020-10-28 | Compagnie Generale Des Etablissements Michelin | Reinforced product comprising a composition comprising a polysulfide compound and tyre comprising said reinforced product |
| FR3087197B1 (en) | 2018-10-11 | 2020-10-23 | Michelin & Cie | RUBBER COMPONENT INCLUDING REINFORCING ELEMENTS |
| WO2020128261A1 (en) | 2018-12-21 | 2020-06-25 | Compagnie Generale Des Etablissements Michelin | Reinforced product comprising a composition containing a polysulphide compound |
| FR3090644A3 (en) | 2018-12-21 | 2020-06-26 | Michelin & Cie | REINFORCED PRODUCT COMPRISING A COMPOSITION COMPRISING A POLYSULFURATED COMPOUND |
| FR3091206A3 (en) | 2018-12-30 | 2020-07-03 | Michelin & Cie | Wire guide block for the production of sheathed reinforcing elements for tires |
| FR3112783B1 (en) | 2020-07-24 | 2023-04-28 | Michelin & Cie | Reinforced product obtained by a process comprising a step of heat treatment of the sheath |
| FR3143032A1 (en) | 2022-12-08 | 2024-06-14 | Compagnie Generale Des Etablissements Michelin | COMPOSITE FOR RUBBER ARTICLE |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4732928A (en) * | 1985-10-02 | 1988-03-22 | Asahi Kasei Kogyo Kabushiki | Highly elastic thermoplastic elastomer composition |
| US4857128A (en) * | 1985-01-18 | 1989-08-15 | Compangnie Generale Des Etablissements Michelin-Michelin Et Cie | Method for making reinforcing assemblies comprising reinforcement threads and a matrix |
| EP0902046A2 (en) * | 1997-09-12 | 1999-03-17 | The Goodyear Tire & Rubber Company | A coated multi-filament reinforcing carbon yarn |
| CN102361746A (en) * | 2009-03-20 | 2012-02-22 | 米其林技术公司 | Self-adhesive composite reinforcement |
| CN102470560A (en) * | 2009-07-31 | 2012-05-23 | 米其林技术公司 | self-adhesive composite reinforcement |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2601293B1 (en) | 1986-07-09 | 1988-11-18 | Michelin & Cie | SHEATHED PIPE FOR TIRE COVERS; PROCESS FOR MAKING THIS TRINGLE; TIRE ENCLOSURES COMPRISING THIS TRINGLE. |
| CA2227525A1 (en) * | 1995-07-26 | 1997-02-13 | Minnesota Mining And Manufacturing Company | Pressure sensitive adhesive patch |
| US5652284A (en) * | 1995-11-09 | 1997-07-29 | Exxon Research & Engineering Company | Thermoplastic elastomer-asphalt nanocomposite composition |
| JP2949331B2 (en) * | 1996-05-30 | 1999-09-13 | 三ツ星ベルト株式会社 | Power transmission V-belt |
| JP3848771B2 (en) * | 1998-01-09 | 2006-11-22 | 横浜ゴム株式会社 | Pneumatic tire |
| EP0962562B1 (en) | 1998-06-05 | 2003-09-03 | W.L. GORE & ASSOCIATES GmbH | Yarn |
| WO2001062514A2 (en) * | 2000-02-25 | 2001-08-30 | Foto-Wear, Inc. | Transferable greeting cards |
| JP2002018843A (en) * | 2000-07-11 | 2002-01-22 | Toray Ind Inc | Prepreg |
| JP2003226798A (en) * | 2002-02-06 | 2003-08-12 | Sumitomo Wiring Syst Ltd | Wear-resistant heat-resistant flame-retardant resin composition and electrical wire covered therewith |
| JP4076381B2 (en) * | 2002-07-05 | 2008-04-16 | 横浜ゴム株式会社 | Thermoplastic elastomer composition |
| JP3786645B2 (en) * | 2003-01-08 | 2006-06-14 | 住友電工スチールワイヤー株式会社 | Coated PC steel stranded wire |
| FR2869618B1 (en) | 2004-04-30 | 2008-10-10 | Michelin Soc Tech | IMPROVED ADHESIVE RUBBER COMPOSITION WITH A METAL REINFORCEMENT. |
| JP4004518B2 (en) * | 2005-10-04 | 2007-11-07 | 横浜ゴム株式会社 | Pneumatic tire using rubber laminate |
| FR2934603B1 (en) * | 2008-08-01 | 2012-12-14 | Michelin Soc Tech | SELF-SWITCHING COMPOSITION FOR PNEUMATIC OBJECT. |
| JP2010053495A (en) * | 2008-08-29 | 2010-03-11 | Yokohama Rubber Co Ltd:The | Steel cord for reinforcing tire, and pneumatic tire using the same |
-
2010
- 2010-09-23 FR FR1057666A patent/FR2965209B1/en not_active Expired - Fee Related
-
2011
- 2011-09-16 KR KR1020137010159A patent/KR101798270B1/en active IP Right Grant
- 2011-09-16 CN CN201180045876.2A patent/CN103140338B/en active Active
- 2011-09-16 BR BR112013005826A patent/BR112013005826A8/en not_active IP Right Cessation
- 2011-09-16 EP EP11757627.2A patent/EP2618976B1/en active Active
- 2011-09-16 US US13/825,926 patent/US20130280511A1/en not_active Abandoned
- 2011-09-16 JP JP2013529617A patent/JP6035570B2/en active Active
- 2011-09-16 WO PCT/EP2011/066113 patent/WO2012038341A1/en active Application Filing
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4857128A (en) * | 1985-01-18 | 1989-08-15 | Compangnie Generale Des Etablissements Michelin-Michelin Et Cie | Method for making reinforcing assemblies comprising reinforcement threads and a matrix |
| US4732928A (en) * | 1985-10-02 | 1988-03-22 | Asahi Kasei Kogyo Kabushiki | Highly elastic thermoplastic elastomer composition |
| EP0902046A2 (en) * | 1997-09-12 | 1999-03-17 | The Goodyear Tire & Rubber Company | A coated multi-filament reinforcing carbon yarn |
| CN102361746A (en) * | 2009-03-20 | 2012-02-22 | 米其林技术公司 | Self-adhesive composite reinforcement |
| CN102470560A (en) * | 2009-07-31 | 2012-05-23 | 米其林技术公司 | self-adhesive composite reinforcement |
Also Published As
| Publication number | Publication date |
|---|---|
| KR101798270B1 (en) | 2017-11-15 |
| JP6035570B2 (en) | 2016-11-30 |
| EP2618976B1 (en) | 2014-05-14 |
| EP2618976A1 (en) | 2013-07-31 |
| WO2012038341A1 (en) | 2012-03-29 |
| FR2965209A1 (en) | 2012-03-30 |
| JP2013542119A (en) | 2013-11-21 |
| US20130280511A1 (en) | 2013-10-24 |
| KR20130108365A (en) | 2013-10-02 |
| CN103140338A (en) | 2013-06-05 |
| FR2965209B1 (en) | 2014-04-18 |
| BR112013005826A8 (en) | 2018-01-02 |
| BR112013005826A2 (en) | 2017-11-14 |
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